FindTrial
Sign In

Ultrasound versus landmark technique for the placement of a tube in the subclavian vein of adults during surgery.

Ultrasound-guided versus landmark technique for infraclavicular subclavian venous cannulation in adult surgical patients: a randomized controlled trial. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/10/095529
Enrollment
110
Registered
2025-10-01
Start date
Unknown
Completion date
Unknown
Last updated
2025-10-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: G939- Disorder of brain, unspecified

Interventions

Intervention1: Ultrasound-guided technique: The USG group will employ a longitudinal in-plane technique for the right-sided infraclavicular approach to subclavian venous cannulation. The operator will

Sponsors

AIIMS New Delhi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adult patients aged 18 to 60 with ASA classification I and II who are undergoing general anesthesia for an elective neurosurgical procedure requiring subclavian vein catheterization will be included in this study.

Exclusion criteria

Exclusion criteria: Patients will be excluded if they are Under 18 or over 60 years old Hemodynamically unstable or in shock SBP less than 60 or on vasoactive drugs Experiencing an infection, inflammation, trauma, or hematoma at the cannulation site Having significant coagulopathy Suffering from morbid obesity, BMI more than 40 Kg per m

Design outcomes

Primary

MeasureTime frame
First-attempt success rateTimepoint: T0 (baseline)- needle insertion T1 (End point)-when needle tip enters the vein—

Secondary

MeasureTime frame
Overall Success RateTimepoint: insert the catheter into the subclavian vein within 5 minutes from initial skin puncture or after a maximum of 3 attempts, whichever occurs first.;Number of attempts (skin punctures)Timepoint: Starting point T0- needle insertion End point T1-confirmation of the needle tip entering the vessel;Number of redirectionsTimepoint: Starting point T0- needle insertion End point T1-confirmation of the needle tip entering the vessel;Cannulation timeTimepoint: Starting point T0- from the start of insertion of the introducer needle End point T1- the return of venous blood into the attached syringe in both groups;Procedural TimeTimepoint: Starting point T0- from the initiation of the introducer needle insertion End point T1- placement of the catheter in both groups;Technical Difficulty scoreTimepoint: after ultrasound-guided catheterization;Incidence of mechanical complicationsTimepoint: Starting point T0- initiation of the cannulation procedure End point T1- confirmation of mechanical complication using chest radiography or ultrasonography—

Countries

India

Contacts

Public ContactDr Niraj Kumar

All India Institute of Medical Sciences, New Delhi

drnirajaiims@gmail.com09013770806

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026